Canonical Allele Identifier: CA1977983979
Gene: SNORD27 HGNC NCBI
SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs2085254852

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855023_62855025del , CM000673.2:g.62855023_62855025del GRCh38
NC_000011.9:g.62622495_62622497del , CM000673.1:g.62622495_62622497del GRCh37
NC_000011.8:g.62379071_62379073del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002563.1:n.63_65del (SNORD27)
NR_003098.1:n.152-83_152-81del (SNHG1)
NR_003098.2:n.149-83_149-81del (SNHG1)
NR_152575.1:n.547-83_547-81del (SNHG1)
NR_152576.1:n.539-83_539-81del (SNHG1)
NR_152577.1:n.148+112_148+114del (SNHG1)
NR_152578.1:n.105+112_105+114del (SNHG1)
NR_152579.1:n.148+112_148+114del (SNHG1)
NR_152580.1:n.148+112_148+114del (SNHG1)
NR_152581.1:n.149-83_149-81del (SNHG1)
NR_152582.1:n.106-83_106-81del (SNHG1)
NR_152583.1:n.148+112_148+114del (SNHG1)
NR_152584.1:n.547-83_547-81del (SNHG1)
NR_152585.1:n.546+112_546+114del (SNHG1)